EP1289987B1 - 4-(2-phenylthiazol-5-yl)1,4-diazabicyclo[3.2.2]nonanederivate, ihre herstellung und therapeutische verwendung - Google Patents

4-(2-phenylthiazol-5-yl)1,4-diazabicyclo[3.2.2]nonanederivate, ihre herstellung und therapeutische verwendung Download PDF

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Publication number
EP1289987B1
EP1289987B1 EP01938362A EP01938362A EP1289987B1 EP 1289987 B1 EP1289987 B1 EP 1289987B1 EP 01938362 A EP01938362 A EP 01938362A EP 01938362 A EP01938362 A EP 01938362A EP 1289987 B1 EP1289987 B1 EP 1289987B1
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Prior art keywords
diazabicyclo
added
mmol
mixture
compound
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French (fr)
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EP1289987A1 (de
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Thierry Gallet
Frédéric Galli
Odile Leclerc
Alistair Lochead
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Sanofi Aventis France
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Sanofi Synthelabo SA
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/08—Bridged systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/08—Antiepileptics; Anticonvulsants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16—Anti-Parkinson drugs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/32—Alcohol-abuse
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/34—Tobacco-abuse
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system

Definitions

  • the compounds of the present invention correspond to the general formula (I) in which R 1 , R 2 , R 3 , R 4 and R 5 each represent, independently of each other, a hydrogen or halogen atom or a nitro, amino, trifluoromethyl, trifluoroalkoxy, cyano, hydroxy group (C 1 -C 6 ) alkyl or (C 1 -C 6 ) alkoxy.
  • the compounds of the invention can exist in the form of bases or addition salts with acids.
  • the compounds of general formula (I) can be prepared by reacting 1,4-diazabicyclo [3.2.2] nonane, of formula (II), with a compound of general formula (III) in which R 1 , R 2 , R 3 , R 4 and R 5 are as defined above, then a cyclization of the latter is carried out in the presence of dimer of 4-methoxyphenylthionophosphine sulfide (Lawesson reagent), or else in the presence of 2,4-bis 2,4-bis (phenylthio) 1,3,2,4-dithiadiphosphetane ( cf. Commun. Synt. 1984, 827).
  • the compounds of general formula (III) are available in trade or are accessible by methods described in the litterature.
  • Example 1 (Compound No. 1).
  • the organic phase is extracted with a 0.1 N aqueous solution of hydrochloric acid, the aqueous phase is made alkaline to pH 10 by addition of a concentrated aqueous solution of sodium hydroxide and extracted with chloroform. The organic phase is dried over sodium sulfate and concentrated under reduced pressure. 0.41 g of product is obtained in solid form. Melting point: 177 ° C.
  • the organic phase is extracted with a 0.1 N aqueous hydrochloric acid solution, the aqueous extraction phase is made alkaline to pH 10 by addition of a concentrated aqueous solution of sodium hydroxide, and extracted with chloroform.
  • the organic phase is dried over sodium sulfate and concentrated under reduced pressure. 0.43 g of product is obtained in the form of an amorphous solid.
  • the organic phase is dried over sodium sulfate, evaporated under reduced pressure and the residue is purified by chromatography on a column of silica gel, eluting with a 90/10 mixture of ethyl acetate and methanol.
  • the product obtained is dissolved in acetone, a solution of oxalic acid in acetone is added and the crystals obtained (0.166 g) are collected by filtration. Melting point: 192-193 ° C.
  • the solvent is evaporated off under reduced pressure and the residue is purified by chromatography on a column of silica gel, eluting with a 95/5 / 0.5 mixture of ethyl acetate, methanol and diethylamine.
  • the product obtained is dissolved in ethanol, added to a solution of oxalic acid in ethanol.
  • the crystals obtained (0.176 g) are collected by filtration. Melting point: 219-222 ° C.
  • the aqueous extraction phase is basified to pH 10 by addition of a concentrated aqueous solution of sodium hydroxide and extracted with chloroform.
  • the organic phase is dried over sodium sulfate and concentrated under reduced pressure. 0.95 g of product are obtained in the form of an oil.
  • the solvent is evaporated off under reduced pressure and the residue is purified by chromatography on a column of silica gel, eluting with a 95/5 / 0.5 mixture of ethyl acetate, methanol and ammonia.
  • the product obtained is dissolved in ethanol and added to a solution of oxalic acid in ethanol.
  • the crystals obtained (0.055 g) are collected by filtration. Melting point: 161-163 ° C.
  • Table 1 which follows illustrates the chemical structures and the physical properties of some compounds of the invention.
  • the compounds of the invention have been the subject of tests which have highlighted their interest as therapeutic substances.
  • the pellet is recovered and homogenized using a Polytron TM mill in 15 volumes of double-distilled water at 4 ° C., then it is centrifuged at 8000 g for 20 min. The pellet is removed and the supernatant and the skin layer ("buffy coat") are centrifuged at 40,000 g for 20 min. The pellet is recovered, it is resuspended with 15 volumes of double-distilled water at 4 ° C. and it is centrifuged again at 40,000 g for 20 min before being stored at -80 ° C.
  • the tissue is thawed slowly and suspended in 5 volumes of buffer.
  • 150 ⁇ l of this membrane suspension are preincubated at 37 ° C. for 30 min, in the dark, in the presence or in the absence of the test compound.
  • the membranes are then incubated for 60 min at 37 ° C., in the dark, in the presence of 50 ⁇ l of [ 3 H] ⁇ -bungarotoxin at 1 nM in a final volume of 250 ⁇ l of 20 mM HEPES buffer.
  • the reaction is stopped by filtration on Whatman GF / C TM filters previously treated for 3 h with 0.05% polyethyleneimine.
  • the filters are rinsed with twice 5 ml of buffer at 4 ° C.
  • the non-specific binding is determined in the presence of ⁇ -bungarotoxin at 1 ⁇ M; non-specific binding represents approximately 60% of the total binding recovered on the filter.
  • the percentage of inhibition of the specific binding of [ 3 H] ⁇ -bungarotoxin is determined, then the IC 50 , concentration of compound which inhibits 50% of the specific binding, is calculated.
  • the IC50 values of the most refined compounds of the invention are are between 0.020 and 0.500 ⁇ M.
  • the compounds of the present invention have also been studied as regards their affinity with respect to nicotinic receptors containing the ⁇ 4 ⁇ 2 subunit according to the methods described by Anderson and Arneric in Eur. J. Pharmacol. 1994, 253 , 261 and by Hall et al. in Brain Res. 1993, 600 , 127.
  • Male Sprague Dawley rats weighing 150 to 200 g are decapitated and the whole brain is quickly removed, homogenized in 15 volumes of 0.32 M sucrose solution at 4 ° C and then centrifuged at 1000 g for 10 min. The pellet is removed and the supernatant is centrifuged at 20,000 g for 20 min at 4 ° C.
  • the pellet is recovered and homogenized using a Polytron TM mill in 15 volumes of double-distilled water at 4 ° C., then it is centrifuged at 8000 g for 20 min. The pellet is eliminated and the supernatant and the skin layer ("buffy coat") are centrifuged at 40,000 g for 20 min, the pellet is recovered, it is resuspended in 15 ml of double-distilled water and it is again centrifuged times at 40,000 g before storing at -80 ° C.
  • the tissue is thawed slowly and suspended in 3 volumes of buffer. 150 ⁇ l of this membrane suspension are incubated at 4 ° C. for 120 min in the presence of 100 ⁇ l of [ 3 H] -cytisine at 1 nM in a final volume of 500 ⁇ l of buffer, in the presence or in the absence of compound to be tested .
  • the reaction is stopped by filtration through Whatman GF / B TM filters previously treated with polyethyleneimine, the filters are rinsed with twice 5 ml of buffer at 4 ° C., and the radioactivity retained on the filter is measured by liquid scintigraphy.
  • non-specific binding is determined in the presence of (-) - nicotine at 10 ⁇ M; non-specific binding represents 75 to 85% of the total binding recovered on the filter.
  • percentage of inhibition of the specific binding of [ 3 H] -cytisine is determined, then the IC 50 is calculated, concentration of compound which inhibits 50% of the specific binding.
  • the IC50 values of the most refined compounds of the invention are are between 1.4 and 4 ⁇ M.
  • the results of various tests suggest the use of the compounds in the treatment or prevention of disorders linked to dysfunction of the nicotinic receptors, in particular in the central nervous system.
  • disorders include cognitive alterations, more specifically memory, but also attentional, linked to Alzheimer's disease, pathological aging (Age Associated Memory Impairment, AAMI), Parkinson's syndrome, trisomy 21 (Down's syndrome), syndrome alcoholic from Korsakoff, with vascular dementias (multiinfarct dementia, MDI).
  • the compounds of the invention could also be useful in the treatment of motor disorders observed in Parkinson's disease or other neurological diseases such as Huntington's chorea, Tourette's syndrome, tardive dyskinesia and hyperkinesia.
  • the compounds of the invention can also constitute a curative or symptomatic treatment of cerebrovascular accidents and cerebral hypoxic episodes. They can be used in cases of psychiatric pathologies: schizophrenia, depression, anxiety, panic attacks, compulsive and obsessive behaviors. They can prevent symptoms due to withdrawal from tobacco, alcohol, various addictive substances, such as cocaine, LSD, cannabis, benzodiazepines.
  • the present invention also relates to pharmaceutical compositions containing an effective dose at least one compound according to the invention, in the basic state or a pharmaceutically acceptable salt or solvate, and mixture, if necessary, with suitable excipients.
  • Said excipients are chosen according to the pharmaceutical form and the desired mode of administration.
  • compositions according to the invention can thus be intended for oral, sublingual administration, subcutaneous, intramuscular, intravenous, topical, intratracheal, intranasal, transdermal, rectal, intraocular.
  • the unit administration forms can be, for example, tablets, capsules, granules, powders, oral or injectable solutions or suspensions, transdermal patches ("patch"), suppositories.
  • patch transdermal patches
  • ointments ointments, lotions and eye drops can be considered.
  • Said unit forms are dosed to allow daily administration of 0.01 to 20 mg of active principle per kg of body weight, depending on the dosage form.
  • a pharmaceutical carrier is added to the active principle, micronized or not, which can be composed of diluents, such as, for example, lactose, microcrystalline cellulose, starch, and formulation adjuvants such as binders, (polyvinylpyrrolidone, hydroxypropylmethylcellulose, etc.), flow agents such as silica, lubricants such as magnesium stearate, stearic acid, glycerol tribehenate, sodium stearyl fumarate. Wetting agents or surfactants such as sodium lauryl sulfate can also be added.
  • the production techniques can be direct compression, dry granulation, wet granulation or hot melting.
  • the tablets can be plain, coated, for example with sucrose, or coated with various polymers or other suitable materials. They can be designed to allow rapid, delayed or prolonged release of the active principle thanks to polymer matrices or to specific polymers used in the coating.
  • the active ingredient is mixed with dry pharmaceutical vehicles (simple mixing, dry or wet granulation, or hot fusion), liquids or semi-solids.
  • dry pharmaceutical vehicles simple mixing, dry or wet granulation, or hot fusion
  • liquids or semi-solids can be hard or soft, film-coated or not, so as to have rapid, prolonged or delayed activity (for example for an enteric form).
  • a composition in the form of syrup or elixir or for administration in the form of drops may contain active ingredient together with a sweetener, preferably caloric, methylparaben or propylparaben like antiseptic, flavoring agent and colorant.
  • a sweetener preferably caloric, methylparaben or propylparaben like antiseptic, flavoring agent and colorant.
  • Water dispersible powders and granules can contain the active ingredient in admixture with dispersion or wetting agents, or agents dispersants like polyvinylpyrrolidone, as well as with sweeteners and flavor correcting agents.
  • Suppositories are used for rectal administration prepared with binders melting at rectal temperature, for example cocoa butter or polyethylene glycols.
  • aqueous suspensions, isotonic saline solutions or sterile injectable solutions containing pharmacologically dispersing and / or wetting agents compatible for example propylene glycol or butylene glycol.
  • the active ingredient can also be formulated in the form of microcapsules, possibly with one or more supports or additives, or with a polymer matrix or with a cyclodextrin (transdermal patches, release forms extended).
  • compositions according to the invention comprise a medium compatible with the skin. They can present themselves especially in the form of aqueous, alcoholic or hydroalcoholic, gels, water-in-oil emulsions or oil-in-water having the appearance of a cream or gel, microemulsions, aerosols, or in the form of vesicular dispersions containing ionic lipids and / or non-ionic. These dosage forms are prepared according to the usual methods of the fields considered.
  • compositions according to the invention may contain, next to a compound of general formula (I), other active ingredients which may be useful in the treatment of the disorders and diseases indicated above.

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  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Neurology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Psychiatry (AREA)
  • Addiction (AREA)
  • Psychology (AREA)
  • Pain & Pain Management (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Cardiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Claims (4)

  1. Verbindung der allgemeinen Formel (I)
    Figure 00170001
    in der
    R1, R2, R3, R4 und R5 jeweils unabhängig voneinander ein Wasserstoffatom oder ein Halogenatom oder eine Nitro-, Amino-, Trifluormethyl-, Trifluoralkoxy-, Cyano-, Hydroxy-, (C1-C6)-Alkyl- oder (C1-C6)-Alkoxygruppe bedeuten, in Form der Base oder der Säureadditionssalze.
  2. Verfahren zur Herstellung einer Verbindung nach Anspruch 1, dadurch gekennzeichnet, daß man 1,4-Diazabicyclo[3.2.2]nonan mit einer Verbindung der allgemeinen Formel (III) umsetzt
    Figure 00170002
    in der R1, R2, R3, R4 und R5 die oben angegebenen Bedeutungen besitzen, dann eine Cyclisierung der erhaltenen Verbindung in Gegenwart des Dimeren des 4-Methoxyphenylthionophosphin-sulfids (Lawesson-Reagens) oder in Gegenwart des 2,4-Disulfids von 2,4-Bis(phenylthio)-1,3,2,4-dithiadiphosphetan bewirkt.
  3. Arzneimittel, dadurch gekennzeichnet, daß es aus einer Verbindung nach Anspruch 1 besteht.
  4. Pharmazeutische Zubereitung, dadurch gekennzeichnet, daß sie eine Verbindung nach Anspruch 1 in Kombination mit einem Trägermaterial enthält.
EP01938362A 2000-05-31 2001-05-29 4-(2-phenylthiazol-5-yl)1,4-diazabicyclo[3.2.2]nonanederivate, ihre herstellung und therapeutische verwendung Expired - Lifetime EP1289987B1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR0006978 2000-05-31
FR0006978A FR2809732B1 (fr) 2000-05-31 2000-05-31 DERIVES DE 4(-2-PHENYLTHIAZOL-5-yl)-1,4-DIAZABICYCLO-[3.2.2] NONANE, LEUR PREPARATION ET LEUR APPLICATION ENTHERAPEUTIQUE
PCT/FR2001/001650 WO2001092260A1 (fr) 2000-05-31 2001-05-29 Derives de 4-(2-phenylthiazol-5-yl)-1,4-diazabicyclo-[3.2.2]nonane, leur preparation et leur application en therapeutique

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EP1289987B1 true EP1289987B1 (de) 2004-05-19

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US (1) US7001902B2 (de)
EP (1) EP1289987B1 (de)
JP (1) JP4939720B2 (de)
AR (1) AR028649A1 (de)
AT (1) ATE267201T1 (de)
AU (1) AU2001264043A1 (de)
DE (1) DE60103394T2 (de)
FR (1) FR2809732B1 (de)
HU (1) HU229600B1 (de)
TW (1) TW591028B (de)
WO (1) WO2001092260A1 (de)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE0000540D0 (sv) 2000-02-18 2000-02-18 Astrazeneca Ab New compounds
FR2832713B1 (fr) * 2001-11-23 2004-02-13 Sanofi Synthelabo Derives de 4-(1,3,4-thiadiazol-2-yl)-1,4-diazabicyclo[3.2.2] nonane, leur preparation et leur application en therapeutique
SE0202430D0 (sv) * 2002-08-14 2002-08-14 Astrazeneca Ab New Compounds
SE0202465D0 (sv) * 2002-08-14 2002-08-14 Astrazeneca Ab New compounds
MXPA05003317A (es) 2002-09-25 2005-07-05 Memory Pharm Corp Indazoles, benzotiazoles y benzoisotiazoles asi como preparacion y usos de los mismos.
EP1785425B1 (de) * 2002-09-30 2009-03-25 NeuroSearch A/S 1,4-Diazabicycloalkanderivate, deren Herstellung und Verwendung
JP4711391B2 (ja) * 2002-09-30 2011-06-29 ニューロサーチ、アクティーゼルスカブ 新規１，４−ジアザビシクロアルカン誘導体及びその製造方法
AU2003280309A1 (en) * 2002-11-11 2004-06-03 Neurosearch A/S 1,4-diazabicyclo (3,2,2)nonane derivatives, preparation and therapeutical use thereof
US7223753B2 (en) 2002-11-11 2007-05-29 Neurosearch A/S Diazabicyclic biaryl derivatives
RU2389729C2 (ru) * 2003-12-22 2010-05-20 Мемори Фармасьютиклз Корпорейшн 1н-индазолы, 1, 2-бензизоксазолы и 1, 2-бензизотиазолы, их получение и применение
JP2007520527A (ja) * 2004-02-04 2007-07-26 ノイロサーチ アクティーゼルスカブ ニコチン性アセチルコリン受容体リガンドとしてのジアザ２環式アリール誘導体
CA2554050A1 (en) 2004-02-04 2005-08-18 Neurosearch A/S Diazabicyclic aryl derivatives as cholinergic receptor modulators
EP1735306A2 (de) 2004-03-25 2006-12-27 Memory Pharmaceuticals Corporation Indazole, benzothiazole, benzoisothiazole, benzisoxazole und deren herstellung und verwendungen
CA2567977A1 (en) 2004-04-22 2006-01-05 Memory Pharmaceutical Corporation Indoles, 1h-indazoles, 1,2-benzisoxazoles, 1,2-benzoisothiazoles, and preparation and uses thereof
NZ551712A (en) * 2004-05-07 2010-07-30 Memory Pharm Corp 1H-indazoles, benzothiazoles, 1,2-benzoisoxazoles, 1,2-benzoisothiazoles, and chromones and preparations and uses thereof
MX2007006743A (es) * 2004-12-15 2007-07-09 Astrazeneca Ab Ligandos del receptor de acetilcolina nicotinica.
CA2591817A1 (en) 2004-12-22 2006-06-29 Memory Pharmaceuticals Corporation Nicotinic alpha-7 receptor ligands and preparation and uses thereof
US7662812B2 (en) 2005-02-16 2010-02-16 Neurosearch A/S Diazabicyclic aryl derivatives and their use as chinolinergic ligands at nicotinic acetylcholine receptors
US8106066B2 (en) 2005-09-23 2012-01-31 Memory Pharmaceuticals Corporation Indazoles, benzothiazoles, benzoisothiazoles, benzisoxazoles, pyrazolopyridines, isothiazolopyridines, and preparation and uses thereof
ATE473978T1 (de) 2005-12-06 2010-07-15 Neurosearch As Neue diazabicyclische arylderivate und medizinische verwendung dafür
WO2007135121A1 (en) 2006-05-23 2007-11-29 Neurosearch A/S Novel 8,10-diaza-bicyclo[4.3.1]decane derivatives and their medical use
WO2007138038A1 (en) * 2006-05-30 2007-12-06 Neurosearch A/S Novel 1,4-diaza-bicyclo[3.2.2]nonyl oxadiazolyl derivatives and their medical use

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IN166416B (de) * 1985-09-18 1990-05-05 Pfizer
NZ226000A (en) * 1987-09-10 1991-06-25 Merck Sharp & Dohme Oxadiazolyl-azabicycloheptanes and pharmaceutical compositions
US5478939A (en) * 1994-07-20 1995-12-26 American Cyanamid Company (R,R) and (S,S) 2,5-diazabicyclo [2,2,1]heptane derivatives
FR2786770B1 (fr) 1998-12-04 2001-01-19 Synthelabo Derives de 1,4-diazabicyclo[3.2.2.]nonane, leur preparation et leur application en therapeutique

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EP1289987A1 (de) 2003-03-12
TW591028B (en) 2004-06-11
AR028649A1 (es) 2003-05-21
US7001902B2 (en) 2006-02-21
AU2001264043A1 (en) 2001-12-11
FR2809732B1 (fr) 2002-07-19
JP2003535090A (ja) 2003-11-25
WO2001092260A1 (fr) 2001-12-06
DE60103394D1 (de) 2004-06-24
FR2809732A1 (fr) 2001-12-07
US20040029884A1 (en) 2004-02-12
JP4939720B2 (ja) 2012-05-30
DE60103394T2 (de) 2005-06-02
HU229600B1 (en) 2014-02-28
HUP0302157A3 (en) 2011-03-28
ATE267201T1 (de) 2004-06-15
HUP0302157A2 (hu) 2003-10-28

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